Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

Sylvie Bannwarth; Samira Ait-El-Mkadem; Annabelle Chaussenot; Emmanuelle C. Genin; Sandra Lacas-Gervais; Konstantina Fragaki; Laetitia Berg-Alonso; Yusuke Kageyama; Valérie Serre; David Moore; Annie Verschueren; Cécile Rouzier; Isabelle Le Ber; Gaëlle Augé; Charlotte Cochaud; Françoise Lespinasse; Karine N'Guyen; Anne De Septenville; Alexis Brice; Patrick Yu-Wai-Man; Hiromi Sesaki; Jean Pouget; Véronique Paquis-Flucklinger

doi:10.1093/brain/awv015

Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Emmanuelle C. Genin, Sandra Lacas-Gervais, Konstantina Fragaki, Laetitia Berg-Alonso, Yusuke Kageyama, Valérie Serre, David Moore, Annie Verschueren, Cécile Rouzier, Isabelle Le Ber, Gaëlle Augé, Charlotte Cochaud, Françoise Lespinasse, Karine N'Guyen, Anne De Septenville, Alexis Brice, Patrick Yu-Wai-ManHiromi Sesaki, Jean Pouget, Véronique Paquis-Flucklinger

School of Medicine

Research output: Contribution to journal › Letter › peer-review

Original language	English (US)
Pages (from-to)	e377
Journal	Brain
Volume	138
Issue number	9
DOIs	https://doi.org/10.1093/brain/awv015
State	Published - Sep 1 2015

ASJC Scopus subject areas

Clinical Neurology

Access to Document

10.1093/brain/awv015

Cite this

Bannwarth, S., Ait-El-Mkadem, S., Chaussenot, A., Genin, E. C., Lacas-Gervais, S., Fragaki, K., Berg-Alonso, L., Kageyama, Y., Serre, V., Moore, D., Verschueren, A., Rouzier, C., Le Ber, I., Augé, G., Cochaud, C., Lespinasse, F., N'Guyen, K., De Septenville, A., Brice, A., ... Paquis-Flucklinger, V. (2015). Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation. Brain, 138(9), e377. https://doi.org/10.1093/brain/awv015

Reply : A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation. / Bannwarth, Sylvie; Ait-El-Mkadem, Samira; Chaussenot, Annabelle; Genin, Emmanuelle C.; Lacas-Gervais, Sandra; Fragaki, Konstantina; Berg-Alonso, Laetitia; Kageyama, Yusuke; Serre, Valérie; Moore, David; Verschueren, Annie; Rouzier, Cécile; Le Ber, Isabelle; Augé, Gaëlle; Cochaud, Charlotte; Lespinasse, Françoise; N'Guyen, Karine; De Septenville, Anne; Brice, Alexis; Yu-Wai-Man, Patrick; Sesaki, Hiromi; Pouget, Jean; Paquis-Flucklinger, Véronique.

In: Brain, Vol. 138, No. 9, 01.09.2015, p. e377.

Research output: Contribution to journal › Letter › peer-review

Bannwarth, S, Ait-El-Mkadem, S, Chaussenot, A, Genin, EC, Lacas-Gervais, S, Fragaki, K, Berg-Alonso, L, Kageyama, Y, Serre, V, Moore, D, Verschueren, A, Rouzier, C, Le Ber, I, Augé, G, Cochaud, C, Lespinasse, F, N'Guyen, K, De Septenville, A, Brice, A, Yu-Wai-Man, P, Sesaki, H, Pouget, J & Paquis-Flucklinger, V 2015, 'Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation', Brain, vol. 138, no. 9, pp. e377. https://doi.org/10.1093/brain/awv015

Bannwarth, Sylvie ; Ait-El-Mkadem, Samira ; Chaussenot, Annabelle ; Genin, Emmanuelle C. ; Lacas-Gervais, Sandra ; Fragaki, Konstantina ; Berg-Alonso, Laetitia ; Kageyama, Yusuke ; Serre, Valérie ; Moore, David ; Verschueren, Annie ; Rouzier, Cécile ; Le Ber, Isabelle ; Augé, Gaëlle ; Cochaud, Charlotte ; Lespinasse, Françoise ; N'Guyen, Karine ; De Septenville, Anne ; Brice, Alexis ; Yu-Wai-Man, Patrick ; Sesaki, Hiromi ; Pouget, Jean ; Paquis-Flucklinger, Véronique. / Reply : A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation. In: Brain. 2015 ; Vol. 138, No. 9. pp. e377.

@article{f317990d4ffa4935a81201e57834808c,

title = "Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation",

author = "Sylvie Bannwarth and Samira Ait-El-Mkadem and Annabelle Chaussenot and Genin, {Emmanuelle C.} and Sandra Lacas-Gervais and Konstantina Fragaki and Laetitia Berg-Alonso and Yusuke Kageyama and Val{\'e}rie Serre and David Moore and Annie Verschueren and C{\'e}cile Rouzier and {Le Ber}, Isabelle and Ga{\"e}lle Aug{\'e} and Charlotte Cochaud and Fran{\c c}oise Lespinasse and Karine N'Guyen and {De Septenville}, Anne and Alexis Brice and Patrick Yu-Wai-Man and Hiromi Sesaki and Jean Pouget and V{\'e}ronique Paquis-Flucklinger",

year = "2015",

month = sep,

day = "1",

doi = "10.1093/brain/awv015",

language = "English (US)",

volume = "138",

pages = "e377",

journal = "Brain",

issn = "0006-8950",

publisher = "Oxford University Press",

number = "9",

}

TY - JOUR

T1 - Reply

T2 - A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

AU - Bannwarth, Sylvie

AU - Ait-El-Mkadem, Samira

AU - Chaussenot, Annabelle

AU - Genin, Emmanuelle C.

AU - Lacas-Gervais, Sandra

AU - Fragaki, Konstantina

AU - Berg-Alonso, Laetitia

AU - Kageyama, Yusuke

AU - Serre, Valérie

AU - Moore, David

AU - Verschueren, Annie

AU - Rouzier, Cécile

AU - Le Ber, Isabelle

AU - Augé, Gaëlle

AU - Cochaud, Charlotte

AU - Lespinasse, Françoise

AU - N'Guyen, Karine

AU - De Septenville, Anne

AU - Brice, Alexis

AU - Yu-Wai-Man, Patrick

AU - Sesaki, Hiromi

AU - Pouget, Jean

AU - Paquis-Flucklinger, Véronique

PY - 2015/9/1

Y1 - 2015/9/1

UR - http://www.scopus.com/inward/record.url?scp=84926411806&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84926411806&partnerID=8YFLogxK

U2 - 10.1093/brain/awv015

DO - 10.1093/brain/awv015

M3 - Letter

C2 - 25681413

AN - SCOPUS:84926411806

VL - 138

SP - e377

JO - Brain

JF - Brain

SN - 0006-8950

IS - 9

ER -